5-Chloro-2-[(3-fluorobenzyl)oxy]benzaldehyde is an organic compound characterized by its aromatic structure, which includes a chloro substituent and a benzaldehyde functional group. The presence of the chloro group introduces a degree of electron-withdrawing character, influencing the compound's reactivity and polarity. The 3-fluorobenzyl ether moiety contributes to the compound's overall hydrophobic character while also providing potential sites for further chemical modification. This compound is likely to exhibit moderate solubility in organic solvents and limited solubility in water due to its hydrophobic characteristics. Its functional groups suggest potential applications in medicinal chemistry, particularly in the synthesis of biologically active compounds or as intermediates in organic synthesis. Additionally, the presence of halogens may impart unique properties, such as increased lipophilicity or altered electronic characteristics, which can be advantageous in drug design. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks if ingested or inhaled.

5-chloro-2-[(3-fluorobenzyl)oxy]benzaldehyde

667437-25-4: 5-Chloro-2-[(3-fluorobenzyl)oxy]benzaldehyde is an organic compound characterized by its aromatic structure, which includes a chloro substituent and a benzaldehyde functional group. The presence of the chloro group introduces a degree of electron-withdrawing character, influencing the compound's reactivity and polarity. The 3-fluorobenzyl ether moiety contributes to the compound's overall hydrophobic character while also providing potential sites for further chemical modification. This compound is likely to exhibit moderate solubility in organic solvents and limited solubility in water due to its hydrophobic characteristics. Its functional groups suggest potential applications in medicinal chemistry, particularly in the synthesis of biologically active compounds or as intermediates in organic synthesis. Additionally, the presence of halogens may impart unique properties, such as increased lipophilicity or altered electronic characteristics, which can be advantageous in drug design. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks if ingested or inhaled.

CAS 667437-25-4

5-chloro-2-[(3-fluorobenzyl)oxy]benzaldehyde

3-Chloro-6-(3′-fluorobenzyloxy)benzaldehyde

Ref: 10-F307569